Snorkel: an epitope tagging system for measuring the surface expression of membrane proteins.

Tags are widely used to monitor a protein's expression level, interactions, protein trafficking, and localization. Membrane proteins are often tagged in their extracellular domains to allow discrimination between protein in the plasma membrane from that in internal pools. Multipass membrane pro...

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Main Authors: Michael Brown, Lewis J Stafford, Dale Onisk, Tony Joaquim, Alhagie Tobb, Larissa Goldman, David Fancy, James Stave, Ross Chambers
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3759426?pdf=render
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spelling doaj-b5d08ce27c714ccba1f616fcfe0008bb2020-11-25T01:34:53ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0189e7325510.1371/journal.pone.0073255Snorkel: an epitope tagging system for measuring the surface expression of membrane proteins.Michael BrownLewis J StaffordDale OniskTony JoaquimAlhagie TobbLarissa GoldmanDavid FancyJames StaveRoss ChambersTags are widely used to monitor a protein's expression level, interactions, protein trafficking, and localization. Membrane proteins are often tagged in their extracellular domains to allow discrimination between protein in the plasma membrane from that in internal pools. Multipass membrane proteins offer special challenges for inserting a tag since the extracellular regions are often composed of small loops and thus inserting an epitope tag risks perturbing the structure, function, or location of the membrane protein. We have developed a novel tagging system called snorkel where a transmembrane domain followed by a tag is appended to the cytoplasmic C-terminus of the membrane protein. In this way the tag is displayed extracellularly, but structurally separate from the membrane protein. We have tested the snorkel tag system on a diverse panel of membrane proteins including GPCRs and ion channels and demonstrated that it reliably allows for monitoring of the surface expression.http://europepmc.org/articles/PMC3759426?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Michael Brown
Lewis J Stafford
Dale Onisk
Tony Joaquim
Alhagie Tobb
Larissa Goldman
David Fancy
James Stave
Ross Chambers
spellingShingle Michael Brown
Lewis J Stafford
Dale Onisk
Tony Joaquim
Alhagie Tobb
Larissa Goldman
David Fancy
James Stave
Ross Chambers
Snorkel: an epitope tagging system for measuring the surface expression of membrane proteins.
PLoS ONE
author_facet Michael Brown
Lewis J Stafford
Dale Onisk
Tony Joaquim
Alhagie Tobb
Larissa Goldman
David Fancy
James Stave
Ross Chambers
author_sort Michael Brown
title Snorkel: an epitope tagging system for measuring the surface expression of membrane proteins.
title_short Snorkel: an epitope tagging system for measuring the surface expression of membrane proteins.
title_full Snorkel: an epitope tagging system for measuring the surface expression of membrane proteins.
title_fullStr Snorkel: an epitope tagging system for measuring the surface expression of membrane proteins.
title_full_unstemmed Snorkel: an epitope tagging system for measuring the surface expression of membrane proteins.
title_sort snorkel: an epitope tagging system for measuring the surface expression of membrane proteins.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description Tags are widely used to monitor a protein's expression level, interactions, protein trafficking, and localization. Membrane proteins are often tagged in their extracellular domains to allow discrimination between protein in the plasma membrane from that in internal pools. Multipass membrane proteins offer special challenges for inserting a tag since the extracellular regions are often composed of small loops and thus inserting an epitope tag risks perturbing the structure, function, or location of the membrane protein. We have developed a novel tagging system called snorkel where a transmembrane domain followed by a tag is appended to the cytoplasmic C-terminus of the membrane protein. In this way the tag is displayed extracellularly, but structurally separate from the membrane protein. We have tested the snorkel tag system on a diverse panel of membrane proteins including GPCRs and ion channels and demonstrated that it reliably allows for monitoring of the surface expression.
url http://europepmc.org/articles/PMC3759426?pdf=render
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